Canonical Allele Identifier: CA337099521
Gene: MT-ND5 HGNC NCBI

Linked Data

ClinVar Variation Id: 693474
ClinVar RCV Id: RCV000854846
dbSNP Id: rs879105366
MyVariant Identifiers: chrMT:g.12662A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12662A>G , J01415.2:m.12662A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361567.2:c.326A>G ENSP00000354813.2:p.Asn109Ser
Search 100 bp 5'
Search 100 bp 3'